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918504-65-1 分子结构
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N-{3-[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluorophenyl}propane-1-sulfonamide

ChemBase编号:72603
分子式:C23H18ClF2N3O3S
平均质量:489.9221264
单一同位素质量:489.07254657
SMILES和InChIs

SMILES:
c1(cnc2c(c1)c(c[nH]2)C(=O)c1c(c(ccc1F)NS(=O)(=O)CCC)F)c1ccc(cc1)Cl
Canonical SMILES:
CCCS(=O)(=O)Nc1ccc(c(c1F)C(=O)c1c[nH]c2c1cc(cn2)c1ccc(cc1)Cl)F
InChI:
InChI=1S/C23H18ClF2N3O3S/c1-2-9-33(31,32)29-19-8-7-18(25)20(21(19)26)22(30)17-12-28-23-16(17)10-14(11-27-23)13-3-5-15(24)6-4-13/h3-8,10-12,29H,2,9H2,1H3,(H,27,28)
InChIKey:
GPXBXXGIAQBQNI-UHFFFAOYSA-N

引用这个纪录

CBID:72603 http://www.chembase.cn/molecule-72603.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
N-{3-[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluorophenyl}propane-1-sulfonamide
IUPAC传统名
vemurafenib
N-{3-[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluorophenyl}propane-1-sulfonamide
别名
N-[3-[[5-(4-Chlorophenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]carbonyl]-2,4-difluorophenyl]-1-propanesulfonamide
PLX 4032
RG 7204
Ro 51-85426
Vemurafenib
RG7204
R7204
RO5185426
PLX-4032
CAS号
918504-65-1
PubChem SID
162037528
PubChem CID
42611257

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID
PubChem 42611257 external link

理论计算性质

理论计算性质

JChem
Acid pKa 7.1725626  质子受体
质子供体 LogD (pH = 5.5) 4.612394 
LogD (pH = 7.4) 4.269431  Log P 4.6224833 
摩尔折射率 121.9691 cm3 极化性 48.621117 Å3
极化表面积 91.92 Å2 可自由旋转的化学键
里宾斯基五规则 true 

分子性质

分子性质

理化性质 安全信息 药理学性质 产品相关信息 生物活性(PubChem)
溶解度
DMSO expand 查看数据来源
保存条件
-20°C expand 查看数据来源
MSDS下载
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作用靶点
B-Raf expand 查看数据来源
成盐信息
Free Base expand 查看数据来源
质检报告
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详细说明

详细说明

Selleck Chemicals Selleck Chemicals TRC TRC
Selleck Chemicals -  S1267 external link
Research Area
Description Malignant melanoma,Colorectal cancer
Protocol
Kinase Assay [1]
RAF kinase activity measurements The kinase activities of wild-type RAF and mutants are determined by measuring phosphorylation of biotinylated-BAD protein. For each enzyme (0.01 ng), 20 μL reactions are carried out in 20 mM Hepes (pH 7.0), 10 mM MgCl2, 1 mM DTT, 0.01% (v/v) Tween-20, 50 nM biotin-BAD protein, and 1 mM ATP at room temperature. Reactions are stopped at 5 min with 5 μL of a solution containing 20 mM Hepes (pH 7.0), 200 mM NaCl, 80 mM EDTA, 0.3% (w/v) bovine serum albumin (BSA). The stop solution also includes phospho-BAD (Ser112) antibody, streptavidin-coated donor beads, and protein A acceptor beads. The antibody and beads are pre-incubated in stop solution in the dark at room temperature for 30 min. The final dilution of antibody is 1/2000 and the final concentration of each bead is 10 μg/mL. The assay plates are incubated at room temperature for one hour and then are read on a PerkinElmer AlphaQuest reader. Mutant activities are the average of two different batches of purified protein assayed in duplicate in three different experiments.
Cell Assay [2]
Cell Lines MALME-3M, Colo829, Colo38, A375, SK-MEL28, and A2058 cells
Concentrations 0–10 μM , dissolved in DMSO
Incubation Time 5 days
Methods Cellular proliferation is evaluated by MTT assay. Briefly, cells are plated in 96-well microtiter plates at a density of 1000 to 5000 cells per well in a volume of 180 μL. PLX4032 is prepared at 10 times the final assay concentration in media containing 1% DMSO. Twenty-four hours after cell plating, 20 μL of the appropriate dilution of PLX4032 are added to plates in duplicate. The plates are assayed for proliferation 6 days after the cells are plated. Percent inhibition is calculated and the IC50 is determined from the regression of a plot of the logarithm of the concentration versus percent inhibition.
Animal Study [2]
Animal Models Mice (athymic nude) xenograft models of LOX, Colo829, and A375 cells
Formulation Formulated as microprecipitated bulk powder (MBP), suspended at the desired concentration in an aqueous vehicle containing 2% Klucel LF, and adjusted to pH 4 with dilute HCl
Doses 12.5 mg/kg–100 mg/kg
Administration Oral gavage twice daily
References
[1] Bollag G, et al. Nature, 2010, 467(7315), 596-599.
[2] Yang H, et al. Cancer Res, 2010, 70(13), 5518-5527.
[3] Prahallad A, et al. Nature, 2012, 483(7387), 100-103.
[4] Kumar A, et al. J Mol Biol, 2005, 348(1), 183-193.
Toronto Research Chemicals -  V118500 external link
Vemurafenib selective BRAFV600E kinase inhibitor; an antitumor agent. Vemurafenib functions by inhibiting the proliferation and mitogen-activated protein/extracellular signal-regulated kinase (ERK) kinase and ERK phosphorylation in a panel of tumor cell l

参考文献

参考文献

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专利

专利

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